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MECLIZINE HYDROCHLORIDE

NDC 70518-1308 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMeclizine Hydrocloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA040659
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (25 mg/1)
Marketing started20180817
Marketing ended20261031
Package count1

External sources

Source: openFDA. Public-domain (CC0).